Pearce E I, Ammerlaan W A, Opstelten D
Department of Biochemistry, University of Hong Kong.
Hybridoma. 1996 Feb;15(1):33-42. doi: 10.1089/hyb.1996.15.33.
HIS50 MAb recognizes a GPI-linked molecule on the surface of rat cells committed to the B lineage but is absent from cells of other hematopoietic lineages. Eukaryotic expression cloning of the cDNA has revealed that HIS50 recognizes a rat homologue of human CD24 and murine HSA. CD24/HSA exists in multiple glycoforms and plays an important role in hematopoietic and neural cell development. HIS50 is significant in that it is the only, presently available, anti-rat CD24/HSA MAb. Furthermore it is the only reported MAb with specificity restricted to B cell forms of CD24. Here we report Western blot analysis of HIS50 antigen (ag). In rat bone marrow HIS50 MAb recognized MW species in the range of 35-70 kDa. These species were shown by immunomagnetic cell sorting to be all derived from the HIS50+ cell subset. In other tissues with varying HIS50 levels as judged by immunostaining, apparent levels of HIS50 ag in the 35-70 kDa range varied accordingly. Thus, Western blot data corresponded to the immunostaining data of HIS50 ag, and the size distribution of B-restricted forms of rat CD24 appeared as wide as that reported for the more extensively expressed forms of human and murine CD24. N-Deglycosylation of cell lysates from lymphoid organs reduced the signal in the 35-70 kDa range, without appearance of lower MW HIS50-reactive species. Thus, unlike certain epitopes on human and murine CD24, HIS50 epitopes appeared (partially) N-linked carbohydrate dependent. The data reported here provide a basis for the further use of HIS50 MAb in studying the role of the highly heterogeneous CD24 molecules in cell development.
HIS50单克隆抗体识别大鼠B细胞系细胞表面的一种糖基磷脂酰肌醇连接分子,而其他造血细胞系细胞表面不存在该分子。cDNA的真核表达克隆显示,HIS50识别人类CD24和小鼠HSA的大鼠同源物。CD24/HSA存在多种糖型,在造血和神经细胞发育中起重要作用。HIS50的重要之处在于它是目前唯一可用的抗大鼠CD24/HSA单克隆抗体。此外,它是唯一报道的特异性限于CD24的B细胞形式的单克隆抗体。在此我们报道HIS50抗原(ag)的蛋白质印迹分析。在大鼠骨髓中,HIS50单克隆抗体识别分子量在35 - 70 kDa范围内的条带。通过免疫磁珠细胞分选显示,这些条带均来自HIS50 +细胞亚群。在通过免疫染色判断的具有不同HIS50水平的其他组织中,35 - 70 kDa范围内HIS50抗原的表观水平相应变化。因此,蛋白质印迹数据与HIS50抗原的免疫染色数据一致,并且大鼠CD24的B细胞限制性形式的大小分布与报道的人类和小鼠CD24更广泛表达形式的大小分布一样宽。来自淋巴器官的细胞裂解物的N - 去糖基化降低了35 - 70 kDa范围内的信号,没有出现更低分子量的HIS50反应性条带。因此,与人类和小鼠CD24上的某些表位不同,HIS50表位似乎(部分)依赖于N - 连接的碳水化合物。本文报道的数据为进一步利用HIS50单克隆抗体研究高度异质性的CD24分子在细胞发育中的作用提供了基础。